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Associate Director Global Labeling Strategy Jobs

IQVIA

Associate Labeling Strategy Director

Durham, NC · On-site

$103K - $288K/yr

The Role: IQVIA is seeking a Associate Director of Regulatory Labeling Strategy to support new ... Global labeling experience to provide labeling strategy support across labeling for CCDS, US, EU ...

IQVIA

Associate Labeling Strategy Director

Durham, NC · On-site

$103K - $288K/yr

The Role: IQVIA is seeking a Associate Director of Regulatory Labeling Strategy to support new ... Global labeling experience to provide labeling strategy support across labeling for CCDS, US, EU ...

Eisai, Inc.

Director, Global Labeling

$188K - $247K/yr

The Director of Global Labeling is a leadership position within the global labeling organization, with the incumbent responsible for shaping and executing global regulatory labeling strategies to ...

Eisai

Director, Global Labeling

$188K - $247K/yr

The Director of Global Labeling is a leadership position within the global labeling organization, with the incumbent responsible for shaping and executing global regulatory labeling strategies to ...

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How much do associate director global labeling strategy jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for associate director global labeling strategy in the United States is $30.53, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $39.18 per hour, depending on experience, location, and employer.

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For Associate Director Global Labeling Strategy jobs, the most frequently searched job titles are:

Associate Director, Global Labeling Lead

Cambridge, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 12 days ago

Job description

Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU)Responsibilities:
  • Provide regulatory expertise and strategic guidance to internal stakeholders to develop and maintain pharmaceutical drug/device labeling.
  • Contribute labeling strategy to regulatory strategies; liaise on evolving submission/negotiation plans.
  • Formulate labeling strategies for new/revised prescribing information and packaging; interpret scientific/medical/regulatory data.
  • Advise on labeling requirements, templates/tools, and Health Authority guidance.
  • Drive CCDS/US/EU labeling strategy and lifecycle management; lead development and maintenance of CCDS, US, and EU labels.
  • Prepare labeling vision for early programs; align stakeholders.
  • Lead global labeling teams and cross-functional projects; resolve conflicts/issues with minimal escalation.
  • Support combination product/drug-device labeling; prepare backup strategies for labeling negotiations.
  • Manage labeling processes/tools/systems, project-manage labeling updates to meet timelines, ensure version control/QC, maintain labeling decision records, and deliver labeling training.
Qualifications & Required/Preferred Skills:
  • 7–10 years biopharmaceutical industry experience; 5–7 years direct global US/EU labeling experience desired.
  • Knowledge of EU/US labeling requirements/guidance; combination product/drug-device labeling preferred.
  • Expertise maintaining Core Data Sheet (CCDS), USPI, and EU SmPC; understanding of SPL format for legacy/PLR labels.
  • Proficiency with Electronic Document Management Systems and end-to-end (E2E) labeling tracking systems.
  • Bachelor’s or Master’s required (advanced scientific/health sciences preferred); leadership/management of direct reports preferred.
Location:

Cambridge, MA (Hybrid)

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